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- NP381882.RAUahmasQxCQ8hJb4wWjUfndD23XYbFUzSlh_Twzh96YM130_assertion type Assertion NP381882.RAUahmasQxCQ8hJb4wWjUfndD23XYbFUzSlh_Twzh96YM130_head.
- NP381882.RAUahmasQxCQ8hJb4wWjUfndD23XYbFUzSlh_Twzh96YM130_assertion description "[Chylomicronemia syndrome presenting in childhood is a rare recessive disorder due to mutations of lipoprotein lipase (LPL) and more rarely of APOC2, APOA5, GPIHBP1 or LMF1 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP381882.RAUahmasQxCQ8hJb4wWjUfndD23XYbFUzSlh_Twzh96YM130_provenance.
- NP381882.RAUahmasQxCQ8hJb4wWjUfndD23XYbFUzSlh_Twzh96YM130_assertion evidence source_evidence_literature NP381882.RAUahmasQxCQ8hJb4wWjUfndD23XYbFUzSlh_Twzh96YM130_provenance.
- NP381882.RAUahmasQxCQ8hJb4wWjUfndD23XYbFUzSlh_Twzh96YM130_assertion SIO_000772 23357145 NP381882.RAUahmasQxCQ8hJb4wWjUfndD23XYbFUzSlh_Twzh96YM130_provenance.
- NP381882.RAUahmasQxCQ8hJb4wWjUfndD23XYbFUzSlh_Twzh96YM130_assertion wasDerivedFrom befree-20140225 NP381882.RAUahmasQxCQ8hJb4wWjUfndD23XYbFUzSlh_Twzh96YM130_provenance.
- NP381882.RAUahmasQxCQ8hJb4wWjUfndD23XYbFUzSlh_Twzh96YM130_assertion wasGeneratedBy ECO_0000203 NP381882.RAUahmasQxCQ8hJb4wWjUfndD23XYbFUzSlh_Twzh96YM130_provenance.